Jaeger Dieter
Department of Biology, Emory University, Atlanta, GA 30322, USA.
J Comput Neurosci. 2003 May-Jun;14(3):311-27. doi: 10.1023/a:1023217111784.
Purkinje cells aligned on the medio-lateral axis share a large proportion of their approximately 175,000 parallel fiber inputs. This arrangement has led to the hypothesis that movement timing is coded in the cerebellum by beams of synchronously active parallel fibers. In computer simulations I show that such synchronous activation leads to a narrow spike cross-correlation between pairs of Purkinje cells. This peak was completely absent when shared parallel fiber input was active in an asynchronous mode. To determine the presence of synchronous parallel fiber beams in vivo I recorded from pairs of Purkinje cells in crus IIa of anesthetized rats. I found a complete absence of precise spike synchronization, even when both cells were strongly modulated in their spike rate by trains of air-puff stimuli to the face. These results indicate that Purkinje cell spiking is not controlled by volleys of synchronous parallel fiber inputs in the conditions examined. Instead, the data support a model by which granule cells primarily control Purkinje cell spiking via dynamic population rate changes.
沿中-外侧轴排列的浦肯野细胞共享其约175,000条平行纤维输入中的很大一部分。这种排列导致了一种假说,即运动时间在小脑中由同步活动的平行纤维束编码。在计算机模拟中,我表明这种同步激活会导致浦肯野细胞对之间出现狭窄的尖峰互相关。当共享的平行纤维输入以异步模式活动时,这个峰值完全不存在。为了确定体内是否存在同步平行纤维束,我在麻醉大鼠的IIa小腿中记录了成对的浦肯野细胞。我发现完全没有精确的尖峰同步,即使两个细胞在受到对面吹气刺激序列强烈调节其尖峰频率时也是如此。这些结果表明,在所研究的条件下,浦肯野细胞的放电不受同步平行纤维输入群峰的控制。相反,数据支持一种模型,即颗粒细胞主要通过动态群体速率变化来控制浦肯野细胞的放电。